Who We Are

Noah Medical is building the future of medical robotics. Our next generation robotic platform targets early diagnosis and treatment of patients across multiple indications.We are looking for exceptional engineers and key team members. Our incredibly talented team of engineers, innovators, and industry leaders bring years of experience from the top healthcare companies in the world, including:Intuitive, Auris, Stryker, Johnson & Johnson, Boston Scientific, Verb Surgical, Mako, Think Surgical, Medtronic, and Hansen. We are looking for talented, motivated and ambitious team members to revolutionize robotic surgery.

About The Team

Join our Quality team at Noah Medical, where you'll play a pivotal role in driving
innovation and product leadership in medical robotics. We're a hands-on,
technical, and solution-oriented, and accountable team, seeking like-minded
individuals to join us. Utilizing a data-driven approach, we tackle challenges
and fuel innovation. Committed to exceeding FDA and international regulatory
standards, we take initiative, optimize processes, and implement agile quality
management systems to foster continuous improvement. Our ultimate goal is to
make a meaningful impact on patients' lives by setting new benchmarks and
breaking barriers in the field of medical robotics. Come join us as we shape
the future together!

A Day In The Life Of Our Junior Design Quality Engineer - SW

Provide hands-on guidance for non-product Software programs follow the
process of Computerized Software Validation and others. Participate in the
design development process of non-product software.

● Review and control the non-product software quality for the R&D, IT, Manufacturing organization and ensure the execution of the strategy.

● Review verification plans, and verification procedures based upon the non-product software requirements ensuring that appropriate statistical techniques are applied.

● Support the development and implementation of quality processes for non-product software, including risk management,validation, and documentation.

● Assist in creating and maintaining non-product software
quality plans, protocols, and reports in alignment with company procedures and
regulatory standards (e.g., FDA 21 CFR Part 820, ISO 13485).

● Participate in software validation activities, including requirement analysis, test case development, and execution of validation protocols.

● Collaborate with cross-functional teams (R&D,IT, Manufacturing) to ensure software tools meet quality and compliance requirements.

● Support both internal and external audits related non-product software. Assist in investigating and documenting software-related issues, non-conformances, and corrective/preventive actions
(CAPA).

● Work collaboratively and efficiently in a fast-paced
environment with minimal supervision and guidance.

● Stay updated on industry trends, regulatory
changes, and best practices in software quality engineering.

● Other QMS activities not specified here and as assigned.

About You

● BS in Computer Science, Software development or other related major.

● Minimum of 2 years of Design Quality Engineering work experience in the medical device, experience in non-product software design development quality experience.

● Familiar with Non-product GxP related software applications (i.e. eQMS, ERP, production quality control software application, off-the-shelf software, embedded software, firmware,SaaS, and hardware/software integration that may indirectly impact product quality.

● Familiar with the process of development, implementation, maintenance, and
retirement of GxP related applications and tools.

● Automation Testing Tools: QTP/UFT, Load Testing tools (LoadRunner and Web Performance Load Tester) Microsoft TFS and MS Visio.

● Analyzed business/technical requirements and developed test plans

● Created manual/automation test cases

● Trained junior testers on test script execution

● Maintained automated scripts for functional testing

● Executed performance testing using LoadRunner/Web
Performance Load Tester

● Performed end-to-end application testing and database
validation

● Documented defects and coordinated resolution with developers

● Generated test performance reports.

● An all-English working environment, good at speaking and writing.

● Prefer:

Experience with software testing tools and methodologies.

Knowledge of programming languages (e.g., Python,Java, C++) or scripting tools.

Exposure to risk management frameworks (e.g., ISO
14971).

Familiar with NC/INV/CAPA process, complaint handling process.